清脆的
反式激活crRNA
计算生物学
生物
计算机科学
检测点注意事项
病毒学
Cas9
遗传学
基因
免疫学
作者
Cailing Lin,Feng Chen,Dongchao Huang,Wenyan Li,Changsheng He,Yingjun Tang,Xueping Li,Can Liu,Liya Han,Yunpeng Yang,Yongchong Zhu,R Chen,Yuanju Shi,Chenglai Xia,Zhibin Yan,Hongli Du,Lizhen Huang
标识
DOI:10.1016/j.bios.2023.115609
摘要
Revolutionary all-in-one RPA-CRISPR assays are rapidly becoming the most sought-after tools for point-of-care testing (POCT) due to their high sensitivity and ease of use. Despite the availability of one-pot methods for specific targets, the development of more efficient methods for new targets remains a significant challenge. In this study, we present a rapid and universal approach to establishing an all-in-one RPA-Cas12a method CORDSv2 based on rational balancing amplification and Cas12a cleavage, which achieves ultrasensitive detection of several targets, including SARS-CoV-2, ASFV, HPV16, and HPV18. CORDSv2 demonstrates a limit of detection (LOD) of 0.6 cp/μL and 100% sensitivity for SARS-CoV-2, comparable to qPCR. Combining with our portable device(hippo-CORDS), it has a visual detection LOD of 6 cp/μL and a sensitivity up to 100% for SARS-CoV-2 and 97% for Ct<35 ASFV samples, surpassing most one-pot visual methods. To simplify and accelerate the process for new targets, we also develop a de novo autodesigner by which the optimal couples of primers and crRNA can be selected rapidly. As a universal all-in-one RPA-CRISPR method for on-site testing, CORDSv2 becomes an attractive choice for rapid and accurate diagnosis in resource-limited settings.
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